Canonical Allele Identifier: PA2828322906
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 438585
ClinVar RCV Id: RCV000656086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356301.1:p.Tyr64Asn
CA414246919
NM_001369372.1:c.190T>A